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Improvements in Lung Function and Height among Cohorts of 6-Year-Olds with Cystic Fibrosis from 1994 to 2012

OBJECTIVE: To characterize spirometry and height changes in cohorts of 6-year-olds with cystic fibrosis (CF). STUDY DESIGN: Global Lung Initiative (GLI) forced expiratory volume in 1 second (FEV(1)), forced vital capacity (FVC) and FEV(1)/FVC and CDC height-for-age (HFA) Z-scores were generated for...

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Publicado en:J Pediatr
Main Authors: VanDevanter, Donald R., Pasta, David J., Konstan, Michael W.
Formato: Artigo
Idioma:Inglês
Publicado: 2014
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC4252623/
https://ncbi.nlm.nih.gov/pubmed/25134852
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jpeds.2014.06.061
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